CN102154636B - Preparation method for p type high transmission rate (100)-oriented LaNiO3 nano film - Google Patents
Preparation method for p type high transmission rate (100)-oriented LaNiO3 nano film Download PDFInfo
- Publication number
- CN102154636B CN102154636B CN201010593790A CN201010593790A CN102154636B CN 102154636 B CN102154636 B CN 102154636B CN 201010593790 A CN201010593790 A CN 201010593790A CN 201010593790 A CN201010593790 A CN 201010593790A CN 102154636 B CN102154636 B CN 102154636B
- Authority
- CN
- China
- Prior art keywords
- film
- preparation
- lanio
- transmission rate
- annealing
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
Images
Landscapes
- Inorganic Compounds Of Heavy Metals (AREA)
- Electrodes Of Semiconductors (AREA)
Abstract
The invention relates to the field of microelectronics and photoelectron materials, in particular to a preparation method for a p type high transmission rate (100)-oriented LaNiO3 nano conductive film. The preparation method comprises the following steps of: weighing lanthanum nitrate and nickel nitrate which serve as solutes in the molar ratio of 1:1, wherein the molar ratio of solvent water to ethanol to citric acid to polyethylene glycol is 200:200:2:1, and the concentration of solution is between 0.08 and 0.20 mol/L; depositing precursor solution on a substrate material, drying and performing thermal treatment; increasing the temperature from 350 DEG C to 450 DEG C at the rate of 10 DEG C/minute under the oxygen atmosphere, pretreating at the temperature of 450 DEG C for 10 minutes, and increasing the temperature to 600 DEG C at the rate of 15 DEG C/minute; and annealing for 20 minutes under the nitrogen atmosphere, wherein the annealing temperature is between 600 and 650 DEG C. By the method, the surface uniformity and the polarization degree of LaNiO3 film electrodes are improved, (100) orientation degree is high, the surface roughness is low, the resistivity is low, and the transmission rate is high.
Description
Technical field
The present invention relates to microelectronics and photoelectron material field, the LaNiO of particularly a kind of P type high-transmission rate (100)-orientation
3The preparation method of nano conductive film.
Background technology
Transparent conductive oxide film has good electrical conductivity, to the high-transmission rate of visible light, and infrared region high-reflectivity and other characteristic of semiconductor; Can be applicable to flat-panel display device; Solar-energy photo-voltaic cell, photo-sensor and photoelectron, fields such as microelectronic device.Up to now, the transparent conductive film of having found mainly is In
2O
3, SnO
2With ZnO that mixes Al and the multicomponent system that combines thereof, in flat-panel monitor, be widely used, but they are n N-type semiconductorN or electrical conductor that p type transparent oxide film seldom.LaNiO as p type conductor
3Therefore film is opaque usually, mainly is because thickness has surpassed 200nm, has limited the application of p type conductor at photoelectric field, yet the p type material is the development of p-n junction structure and transparent semiconductor device thereof possibility is provided.Can improve transsmissivity though reduce thickness, reduce thickness and can bring the film surface defective to increase, thereby bring resistivity to raise, this problem is at the LaNiO of sol-gel method preparation
3More outstanding in the film.
LaNiO
3Material has calcium titanium ore structure, is one of preferred material of ferroelectric membranc lower conducting dome, mainly is because LaNiO
3Unit cell parameters (a=0. 382nm) and ferroelectric membranc very approaching, make it not only to can be used as electrode materials, also can be used as structure and performance that inculating crystal layer is optimized ferroelectric membranc.Yet, the LaNiO that different processes obtains
3The surfaceness of film is bigger, and it is inhomogeneous to polarize, and resistivity is high, and is also influential to the performance of ferroelectric membranc, for example can increase the leakage current and the coercive field of upper strata PZT ferroelectric membranc, reduces the residual polarization value, the equal and LaNiO of these factors
3The surfaceness of electrode is relevant with orientation degree.
Summary of the invention
In order to overcome the above problems, to the invention provides and a kind ofly can improve LaNiO
3The LaNiO of the p type high-transmission rate (100) of the surfaceness of electrode and orientation degree-orientation
3The preparation method of film.
The present invention realizes through following measure:
The LaNiO of a kind of p type high-transmission rate (100)-orientation
3The preparation method of film, adopt following steps:
(1) preparation of precursor solution: adopt sol-gel method; 1:1 takes by weighing Lanthanum trinitrate and nickelous nitrate as solute in molar ratio; Be dissolved in mol ratio 1:1 blended water and the ethanol, add Hydrocerol A and polyoxyethylene glycol, water: ethanol: Hydrocerol A: the polyoxyethylene glycol mol ratio is=200:200:2:1; Be mixed with precursor solution, strength of solution is 0.08~0.20mol/L;
(2) LaNiO
3The preparation of thin-film material: adopt annealing process layer by layer; With spin-coating method precursor solution is deposited on the substrate material earlier, then material is placed on oven dry about 250 ℃ on the hot plate, the exsiccant film is placed quick anneal oven thermal treatment; Thermal treatment process is characterised in that: under oxygen atmosphere, be warmed up to 450 ℃ from 350 ℃ of speed with 10 ℃/minute; 450 ℃ of pre-treatment 10min are warmed up to 600 ℃ with 15 ℃/minute speed again, and annealing is 20 minutes under nitrogen atmosphere; Annealing temperature is 600 ℃~650 ℃, obtains LaNiO
3Film.
Annealing is meant the demand according to different application between 600 ℃ to 650 ℃, can select 600 ℃; 625 ℃, to anneal respectively 20 minutes for 650 ℃, each sheet kept 20 minutes on a temperature; 600 ℃ of grain-sizes that obtain are less, and 650 ℃ of grain-sizes that obtain are bigger.
Prepared LaNiO
3Film thickness is less than 50nm, and resistivity is 1 * 10
-4Cm~2 * 10
-4Cm, surfaceness is not more than 1nm.
Substrate material can be selected quartz, glass, silicon chip or sheet metal for use, and sheet metal is Ni sheet or Cu sheet.
The present invention places very thin film on the substrate material, and researcher is with the lower conducting dome of thicker film as device usually, does not notice LaNiO
3The hole on lower conducting dome surface and crackle etc. are to the influence of film electric property and optical property.Therefore, through to pretreatment temperature, annealing temperature, the control of film bed thickness, we have obtained nanometer grade thickness, and orientation degree is high, and surfaceness is little, and resistivity is low, (100) that transsmissivity is high-orientation LaNiO
3Nano-film electrode.
The invention has the beneficial effects as follows: through controlling and adopting only pretreatment temperature, annealing temperature has improved LaNiO
3The surface uniformity of membrane electrode and degree of polarization, orientation degree is high, and surfaceness is little, and resistivity is low; And, obtain p type (the 100)-orientation LaNiO of high-transmission rate through the control of bed thickness
3Nano-film electrode has good practical prospect in the photoelectric device in future.
Description of drawings
Accompanying drawing 1 is embodiment 1 a heat treatment process thetagram;
The LaNiO that accompanying drawing 2 obtains for embodiment 1
3The film atom is tried hard to;
The LaNiO that accompanying drawing 3 obtains for embodiment 1
3The transsmissivity of film under visible light;
The LaNiO of accompanying drawing 4 on the Si substrate, obtaining
3The XRD spectrum of film.
Embodiment
Do bright specifically below in conjunction with specific embodiment to the present invention.
Embodiment 1
Present embodiment is a kind of LaNiO that is used for high-transmission rate (the 100)-orientation of photoelectric device
3Nano-film electrode.
The preparation method of above-mentioned membrane electrode is:
(1) preparation of precursor solution: adopt sol-gel method; 1:1 takes by weighing Lanthanum trinitrate and nickelous nitrate in molar ratio; Being dissolved in mol ratio is in the water and ethanol of 1:1, adds a small amount of Hydrocerol A and polyoxyethylene glycol again, is mixed with precursor solution; Strength of solution is 0.08mol/L, and wherein the mol ratio of solvent is a water: ethanol: Hydrocerol A: polyoxyethylene glycol=200:200:2:1;
(2) LaNiO
3The preparation of thin-film material: adopt annealing process layer by layer; With spin-coating method precursor solution is deposited on the quartz substrate material earlier, material is placed on the hot plate dries then, the exsiccant film is placed quick anneal oven thermal treatment; Thermal treatment process is characterised in that: under oxygen atmosphere, be warmed up to 450 ℃ from 350 ℃ of speed with 10 ℃/minute; 450 ℃ of pre-treatment 10 minutes are warmed up to 600 ℃ with 15 ℃/minute speed again, and annealing is 20 minutes under nitrogen atmosphere; Temperature is 600 ℃, obtains dense film.Use sem to record thickness and be 10nm, the surfaceness of using AFM to record is 0.630nm, and using the four point probe tester to record resistivity is 2 * 10
-4Cm, the heat treatment process temperature curve is as shown in Figure 1.Fig. 2 tries hard to for the atom of the film that present embodiment obtains, and the roughness of film is 0.630nm.Fig. 3 is the transsmissivity figure of present embodiment, can find out that transsmissivity is greater than 80% in visible wavelength range.
Difference according to using can repeat the film that above step obtains target thickness.
Embodiment 2
Present embodiment is a kind of LaNiO that is used for high-transmission rate (the 100)-orientation of photoelectric device
3Nano-film electrode.
The preparation method of above-mentioned membrane electrode is:
(1) preparation of precursor solution: adopt sol-gel method; 1:1 takes by weighing Lanthanum trinitrate and nickelous nitrate in molar ratio; Being dissolved in mol ratio is in the water and ethanol of 1:1, adds a small amount of Hydrocerol A and polyoxyethylene glycol again, is mixed with precursor solution; Strength of solution is 0.20mol/L, and wherein the mol ratio of solvent is a water: ethanol: Hydrocerol A: polyoxyethylene glycol=200:200:2:1;
(2) LaNiO
3The preparation of thin-film material: adopt annealing process layer by layer; With spin-coating method precursor solution is deposited on the silicon substrate material earlier, material is placed on the hot plate dries then, the exsiccant film is placed quick anneal oven thermal treatment; Thermal treatment process is characterised in that: under oxygen atmosphere, be warmed up to 450 ℃ from 350 ℃ of speed with 10 ℃/minute; 10 ℃ of 450 ℃ of pre-treatment are warmed up to 600 ℃ with 15 ℃/minute speed again, and annealing is 20 minutes under nitrogen atmosphere; Annealing temperature is 650 ℃, obtains dense film.Use sem to record thickness and be 25nm, use AFM to record roughness and be 1.000nm, using the four point probe tester to record resistivity is 1 * 10
-4Cm.
The LaNiO of accompanying drawing 4 on the Si substrate, obtaining
3The XRD spectra of film, as can be seen from the figure resulting nano thin-film orientation degree is very high.
Difference according to using can repeat the film that above step obtains target thickness.
Experimental example 3
Present embodiment is a kind of LaNiO that is used for high-transmission rate (the 100)-orientation of photoelectric device
3Nano-film electrode through regulating different strength of solution, obtains the film of different thickness.
The preparation method of above-mentioned membrane electrode is:
(1) preparation of precursor solution: adopt sol-gel method; 1:1 takes by weighing Lanthanum trinitrate and nickelous nitrate in molar ratio; Being dissolved in mol ratio is in the water and ethanol of 1:1, adds a small amount of Hydrocerol A and polyoxyethylene glycol again, is mixed with precursor solution; Strength of solution is 0.10mol/L, and wherein the mol ratio of solvent is a water: ethanol: Hydrocerol A: polyoxyethylene glycol=200:200:2:1;
(2) LaNiO
3The preparation of thin-film material: adopt annealing process layer by layer; With spin-coating method precursor solution is deposited on the substrate material earlier, material is placed on the hot plate dries then, the exsiccant film is placed quick anneal oven thermal treatment; Thermal treatment process is characterised in that: under oxygen atmosphere, be warmed up to 450 ℃ from 350 ℃ of speed with 10 ℃/minute; 10 ℃ of 450 ℃ of pre-treatment are warmed up to 600 ℃ with 15 ℃/minute speed again, and annealing is 20 minutes under nitrogen atmosphere; Annealing temperature is 620 ℃, obtains dense film.Use sem to record thickness and be 12nm, use AFM to record roughness and be 0.7000nm, using the four point probe tester to record resistivity is 1.8 * 10
-4Cm.
Difference according to using can repeat the film that above step obtains target thickness.
Experimental example 4
Present embodiment is a kind of LaNiO that is used for high-transmission rate (the 100)-orientation of photoelectric device
3Nano-film electrode through regulating different strength of solution, obtains the film of different thickness.
The preparation method of above-mentioned membrane electrode is:
(1) preparation of precursor solution: adopt sol-gel method; 1:1 takes by weighing Lanthanum trinitrate and nickelous nitrate in molar ratio; Being dissolved in mol ratio is in the water and ethanol of 1:1, adds a small amount of Hydrocerol A and polyoxyethylene glycol again, is mixed with precursor solution; Strength of solution is 0.15mol/L, and wherein the mol ratio of solvent is a water: ethanol: Hydrocerol A: polyoxyethylene glycol=200:200:2:1;
(2) LaNiO
3The preparation of thin-film material: adopt annealing process layer by layer; With spin-coating method precursor solution is deposited on the substrate material earlier, material is placed on the hot plate dries then, the exsiccant film is placed quick anneal oven thermal treatment; Thermal treatment process is characterised in that: under oxygen atmosphere, be warmed up to 450 ℃ from 350 ℃ of speed with 10 ℃/minute; 10 ℃ of 450 ℃ of pre-treatment are warmed up to 600 ℃ with 15 ℃/minute speed again, and annealing is 20 minutes under nitrogen atmosphere; Annealing temperature is 630 ℃, obtains dense film.Use sem to record thickness and be 17nm, the surfaceness that AFM records is 0.850nm, and using the four point probe tester to record resistivity is 1.3 * 10
-4Cm.
Difference according to using can repeat the film that above step obtains target thickness.
Claims (3)
1. the LaNiO of a p type high-transmission rate (100)-orientation
3The preparation method of film is characterized in that adopting following steps:
(1) preparation of precursor solution: adopt sol-gel method; 1:1 takes by weighing Lanthanum trinitrate and nickelous nitrate as solute in molar ratio; Be dissolved in mol ratio 1:1 blended water and the ethanol, add Hydrocerol A and polyoxyethylene glycol, be mixed with precursor solution; Solvent mol ratio water: ethanol: Hydrocerol A: polyoxyethylene glycol is=200:200:2:1 that strength of solution is 0.08~0.20mol/L;
(2) LaNiO
3The preparation of thin-film material: adopt annealing process layer by layer; With spin-coating method precursor solution is deposited on the substrate material earlier, material is placed on the hot plate dries then, the exsiccant film is placed quick anneal oven thermal treatment; Thermal treatment process is characterised in that: under oxygen atmosphere, be warmed up to 450 ℃ from 350 ℃ of speed with 10 ℃/minute; 450 ℃ of pre-treatment 10min are warmed up to 600 ℃ with 15 ℃/minute speed again, and annealing is 20 minutes under nitrogen atmosphere; Annealing temperature is 600 ℃~650 ℃, obtains LaNiO
3Film.
2. method according to claim 1 is characterized in that prepared LaNiO
3Film thickness is less than 50nm, and resistivity is 1 * 10
-4Cm~2 * 10
-4Cm, surfaceness is not more than 1nm.
3. method according to claim 1 and 2 is characterized in that substrate material is quartz, glass, silicon chip or sheet metal, and said sheet metal is Ni sheet or Cu sheet.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201010593790A CN102154636B (en) | 2010-12-17 | 2010-12-17 | Preparation method for p type high transmission rate (100)-oriented LaNiO3 nano film |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201010593790A CN102154636B (en) | 2010-12-17 | 2010-12-17 | Preparation method for p type high transmission rate (100)-oriented LaNiO3 nano film |
Publications (2)
Publication Number | Publication Date |
---|---|
CN102154636A CN102154636A (en) | 2011-08-17 |
CN102154636B true CN102154636B (en) | 2012-09-12 |
Family
ID=44436299
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201010593790A Expired - Fee Related CN102154636B (en) | 2010-12-17 | 2010-12-17 | Preparation method for p type high transmission rate (100)-oriented LaNiO3 nano film |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN102154636B (en) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102810483B (en) * | 2012-08-07 | 2015-09-23 | 清华大学 | Oxide semiconductor thin-film and preparation method, thin-film transistor and preparation method |
JP6075144B2 (en) * | 2013-03-25 | 2017-02-08 | 三菱マテリアル株式会社 | Composition for forming LaNiO3 thin film and method for forming LaNiO3 thin film using this composition |
JP5754539B2 (en) * | 2013-10-15 | 2015-07-29 | 三菱マテリアル株式会社 | Composition for forming LaNiO3 thin film and method for forming LaNiO3 thin film using this composition |
JP6365294B2 (en) * | 2014-03-25 | 2018-08-01 | 三菱マテリアル株式会社 | Method for forming LaNiO3 thin film |
CN108565127B (en) * | 2018-03-26 | 2021-01-26 | 云南大学 | Electrode material capable of improving specific capacity of supercapacitor, preparation method and application |
CN112062568A (en) * | 2020-09-17 | 2020-12-11 | 广西大学 | Preparation method of PLZST-based film by utilizing thermal strain to induce wide temperature zone electrocaloric effect |
CN115895656B (en) * | 2021-08-24 | 2024-05-03 | 浙江理工大学 | Photoluminescent terbium-doped tin oxide film and preparation method thereof |
CN114231951A (en) * | 2021-11-24 | 2022-03-25 | 江苏籽硕科技有限公司 | Method for preparing LaNiO by using polymer auxiliary deposition method3Method for extending conductive film |
CN115084318B (en) * | 2022-07-18 | 2023-06-09 | 西南科技大学 | Inorganic perovskite type LaNiO 3 Preparation and application of visible photoconductive film |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1721066A (en) * | 2005-05-20 | 2006-01-18 | 济南大学 | Catalyst for lowering combustion temperature of soot in diesel exhaust gas and preparation method thereof |
CN101538156A (en) * | 2009-04-30 | 2009-09-23 | 哈尔滨工业大学 | Preparation method of induced texture ferroelectric film at buffer layer |
US7727322B2 (en) * | 2004-09-17 | 2010-06-01 | Seiko Epson Corporation | Precursor solution, method for manufacturing precursor solution, PZTN compound oxide, method for manufacturing PZTN compound oxide, piezoelectric element, ink jet printer, ferroelectric capacitor, and ferroelectric memory |
CN101811889A (en) * | 2010-04-27 | 2010-08-25 | 济南大学 | Lanthanide-doped bismuth titanate film and preparation method thereof |
CN101863679A (en) * | 2009-04-14 | 2010-10-20 | 中国科学院合肥物质科学研究院 | Method for preparing lanthanum nickel oxide thin-film material |
-
2010
- 2010-12-17 CN CN201010593790A patent/CN102154636B/en not_active Expired - Fee Related
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7727322B2 (en) * | 2004-09-17 | 2010-06-01 | Seiko Epson Corporation | Precursor solution, method for manufacturing precursor solution, PZTN compound oxide, method for manufacturing PZTN compound oxide, piezoelectric element, ink jet printer, ferroelectric capacitor, and ferroelectric memory |
CN1721066A (en) * | 2005-05-20 | 2006-01-18 | 济南大学 | Catalyst for lowering combustion temperature of soot in diesel exhaust gas and preparation method thereof |
CN101863679A (en) * | 2009-04-14 | 2010-10-20 | 中国科学院合肥物质科学研究院 | Method for preparing lanthanum nickel oxide thin-film material |
CN101538156A (en) * | 2009-04-30 | 2009-09-23 | 哈尔滨工业大学 | Preparation method of induced texture ferroelectric film at buffer layer |
CN101811889A (en) * | 2010-04-27 | 2010-08-25 | 济南大学 | Lanthanide-doped bismuth titanate film and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
CN102154636A (en) | 2011-08-17 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN102154636B (en) | Preparation method for p type high transmission rate (100)-oriented LaNiO3 nano film | |
Machado et al. | Band Gap Tuning of Solution-Processed Ferroelectric Perovskite BiFe1–x Co x O3 Thin Films | |
Miao et al. | Continuous electrical tuning of the chemical composition of TaO x-based memristors | |
de Cesare et al. | Electrical properties of ITO/crystalline-silicon contact at different deposition temperatures | |
CN104134720A (en) | Preparation method of organic and inorganic hybridization perovskite material growing by single-source flash evaporation method and plane solar cell of material | |
CN103779425B (en) | A kind of indium gallium zinc oxide semiconductive thin film and indium gallium zinc oxide TFT preparation method | |
Schlipf et al. | Top-down approaches towards single crystal perovskite solar cells | |
Wang et al. | Combustion Synthesis of p-Type Transparent Conducting CuCrO2+ x and Cu: CrO x Thin Films at 180° C | |
Farag et al. | Electrical performance and interface states studies of undoped and Zn-doped CdO/p-Si heterojunction devices | |
CN104916785A (en) | CH3NH3PbI3 thin-film solar cell preparation method | |
Kim et al. | Highly dense and stable p-type thin-film transistor based on atomic layer deposition SnO fabricated by two-step crystallization | |
Wu et al. | Fabricate heterojunction diode by using the modified spray pyrolysis method to deposit nickel–lithium oxide on indium tin oxide substrate | |
CN102176472A (en) | Bulk effect solar cell material and preparation method thereof | |
Pintor-Monroy et al. | Controlling carrier type and concentration in NiO films to enable in situ PN homojunctions | |
Tutsch et al. | The sputter deposition of broadband transparent and highly conductive cerium and hydrogen co‐doped indium oxide and its transfer to silicon heterojunction solar cells | |
CN103078013A (en) | Method for preparing bismuth vanadate/bismuth ferrite heterojunction film solar cells | |
Shi et al. | Significantly improving the crystal growth of a Cu2ZnSn (S, Se) 4 absorber layer by air-annealing a Cu2ZnSnS4 precursor thin film | |
CN108101381A (en) | A kind of bismuthino halide perovskite nanometer sheet and preparation method thereof | |
CN103360107B (en) | A kind of gold-nickel acid lanthanum composite conductive thin film material and preparation method thereof | |
Khambunkoed et al. | Fully-covered slot-die-coated ZnO thin films for reproducible carbon-based perovskite solar cells | |
Gao et al. | Effective passivation and tunneling hybrid a-SiO x (In) layer in ITO/n-Si heterojunction photovoltaic device | |
Ding et al. | Boron Spin-On Doping for Poly-Si/SiO x Passivating Contacts | |
CN107910030A (en) | A kind of preparation method of flexibility BNT ferroelectric thin films | |
CN103325942B (en) | Ferroelectric tunnel junction device | |
Rath et al. | Artificial aging of thin films of the indium-free transparent conducting oxide SrVO3 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20120912 Termination date: 20141217 |
|
EXPY | Termination of patent right or utility model |